## Abstract ^1^H NMR spectra of 26 substituted chalcones (3‐aryl‐1 phenyl‐2‐propene‐1‐ones and 1‐aryl‐3‐phenyl‐2‐propene‐1‐ones) have been studied. The chemical shifts of the α and β protons to the carbonyl group were correlated with Hammett s̀ parameters. To gain information on the effect of the t
Effect of methyl substituents on the NMR spectra of aromatic protons of some nitrobenzene derivatives
✍ Scribed by Paolo Beltrame; Paolo Carniti; Adolfo Lai; Paolo Viglino
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 176 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Proton NMR spectra were recorded and analysed for 1‐bromo‐4‐nitrobenzene, 2‐bromo‐5‐nitroluene, 3‐bromo‐6‐nitrotoluene and 2‐bromo‐5‐nitro‐p‐xylene, as well as for the corresponding compounds having p‐CH~3~C~6~H~4~S in place of Br. Chemical shifts and coupling constants generally agree with expected values; however, a deshielding effect of the methyl group on aromatic protons was observed in one case.
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